- Marine Record
- Open Access
First records of two Padina species (Dictyotales, Phaeophyceae) from the Syrian coast (eastern Mediterranean)
Marine Biodiversity Records volume 9, Article number: 93 (2016)
Padina ditristromatica and Padina boryana (Dictyotales, Phaeophyceae) are recorded for the first time from the Syrian coast (eastern Mediterranean). Padina ditristromatica has been previously reported in the west and the north east of the Mediterranean (Ni-Ni-Win et al. 2011) and Padina boryana from the southern Mediterranean (Geraldino et al. 2005). The morphological and anatomical characteristics have been used to confirm the new Padina spp.
Marine macrophytes have been thoroughly studied in the western Mediterranean, but there are fewer studies for the eastern Mediterranean (Giaccone 1968; Mayhoob 1976; UNEP/IUCN/GIS 1990) especially of the Phaeophycean algae (Mayhoob 1989, 2004; Mayhoob and Billard 1991; Mayhoob and Hatoum 2005).
Specimens of the genus Padina Adanson were collected from Syria during a survey of Phaeophyceae.
This genus includes about 27 species (Papenfuss 1977) in tropical and sub-tropical waters. In the Mediterranean Sea only 5 species have been reported: Padina pavonica (L) Thivy, P. boryana Thivy (Ribera et al. 1992), P. antillarum (Kützing) Piccone (P. tetrastromatica Hauck (Mayhoob 2004)), P. ditristromatica Ni-Ni-Win & H. and P. pavonicoides Ni-Ni-Win & H. Kawai (Ni-Ni-Win et al. 2011; Cormaci et al. 2012). Two of these are found on the Syrian coast: P. pavonica and P. tetrastromatica (Mayhoob 2004).
This paper describes the recording of 2 species of the brown alga genus Padina (Dictyotales, Phaeophyceae) for the first time on the Syrian coast.
Materials and methods
Samples were collected from 2 sites: Al-madinah Al-riadiah (35° 17ʹ 38.07″ N, 35° 55ʹ 23.71″ E) and the coast of Tal Socass (35° 17ʹ 54.86″ N, 35° 55ʹ 17.67″ E) in spring-summer 2014 from the lower intertidal zone at a depth of 2 m. The samples were washed thoroughly and preserved in a 4 % formalin-seawater solution for further investigation. Some of these samples were preserved in the form of herbarium sheets and given series numbers with the date of collection. They were kept in the herbarium of the High Institute of Marine Researches (Latakia, Syria).
Transverse sections were made by freehand cutting with the help of shaving blades.
Twenty preserved specimens of Padina boryana and 50 specimens of Padina ditristromatica were studied morphologically and anatomically.
Padina boryana Thivy
The thalli are yellowish brown in colour, and are moderately calcified on the lower surface (opposite the inrolled margin), especially at the stipe and lightly calcified on the upper surface (facing the inrolled margin). They are composed of fan-shaped blades with rhizoids forming the holdfast (Fig. 1a). The erect thalli are up to 7 cm in height. The sporangial rows alternate with hair rows at different intervals only on the upper surface of the thallus.
A transverse section of the thallus shows 2 layers of cells (Fig. 1b). The outer cells are small and nearly square, measuring 36 μm in length. The inner cells are large and rectangular in shape, measuring 58 μm in length. The sporangial sori and hair lines are close to each other (Fig. 1d). The sporangial sori are not covered with an indusium.
Padina ditristromatica Ni-Ni-Win & H. Kawai
The thalli are composed of fan-shaped lobes with inrolled margins. These lobes are attached to each other at the base by a short stem (Fig. 2a).
The thallus is yellowish or greenish-brown between 5 and 10 cm high and moderately calcified on both surfaces.
On the lower surface of the thallus a number of semicircular lines of 2 different types can be seen: reproductive sori (the larger and darker lines) and hair lines. The reproductive sori were found only on the lower surface and formed a single line of separated dark spots (Fig. 2b). And they are successive at equal distance.
The reproductive sori and the hair lines are close to each other or may be merged into single lines (Fig. 2b).
Hair lines were found on the lower and upper surface of the thallus alternating between the 2 surfaces (Fig. 2b). The long fibrous hairs are only on the lower surface of stem of the thallus. The ‘Vaughaniella’ stage was not found in this species.
The oogonial sori are located near to the hair lines (Fig. 2b) and formed spots in narrow lines only on the lower surface (Fig. 2a). Each 1 of them is surrounded by an indusium (Fig. 2d). The mature oogonium has a spherical shape and is 100 μm in diameter (Fig. 2e).
According to the morphological and anatomical observations of these specimens and previous research (Gaillard 1967; Geraldino et al. 2005; Coppejans et al. 2009; Ni-Ni-Win et al. 2011; Abbas and Shameel 2013) the species are identified as P. boryana Thivy and P. ditristromatica Ni-Ni-Win & H. Kawai.
They are clearly distinguished from each other in terms of morphological and anatomical characteristics, mainly in the numbers of cell layers in the thallus, the degree of calcification on the thallus surface, and the structure of the reproductive sori.
P. pavonica is mostly 3 layers thick and occasionally 4 layers at the base of the thallus (Taylor 1960; Ni-Ni-Win et al. 2011), but there is a mixture of 2 and three layers in P. ditristromatica (Ni-Ni-Win et al. 2011; this study).
Padina ditristromatica is similar to P. tetrastromatica Hauck in respect of the dioecious gametophyte and the presence of an indusium (Gaillard 1967; Ni-Ni-Win et al. 2011; this study) (Table 1), but they differ in the numbers of cell layers in the thallus (Table 1) where P. tetrastromatica is mostly 4 layers thick (Gaillard 1967).
In addition, P. ditristromatica is different from P. pavonica and P. tetrastromatica in terms of the structure and arrangement of sporangial sori which in this species are located distally and adjacent to the hair lines only on the lower surface (Ni-Ni-Win et al. 2011). Mean while in P. pavonica and P. tetrastromatica they are located in concentric rows girdling the hair lines on both surfaces (Taylor 1960; Gaillard 1967; Ni-Ni-Win et al. 2011).
Padina pavonicoides is different from P. ditristromatica in that its thallus is composed of 3 cell layers from the base to the marginal portion and 2 layers at the inrolled margin and by the alternating hair lines that are spaced at equal distances between the upper and lower surfaces (Ni-Ni-Win et al. 2011).
Padina boryana differs from P. ditristromatica in terms of the number of cell layers in that it is mostly 2-layers thick throughout the thallus and it also lacks an indusium (Farrant and King 1989; Geraldino et al. 2005; this study) (Table 1).
Marine vegetation in the eastern Mediterranean, including the coast of Syria, belongs to the Atlantic-Mediterranean province (Giaccone 1968; Mayhoob, 1976). However, some circumtropical species are establishing permanent populations so that some tropical characteristics can be attributed to this region.
According to the world-wide distribution of these 2 species and the lack of information concerning the biodiversity of macroalgae in the eastern Mediterranean they might be endemic, relics of the Sea of Tethys, or alien species that have recently been introduced to the Mediterranean sea (Occhipinti-Ambrogi 2000; Boudouresque and Verlaque 2002; Streftaris et al. 2005, 2007; Galil and Zenetos 2008).
Abbas A, Shameel M. Morpho-anatomical studies on the genus Padina (Dictyotales, Phaeophycota) from the Coast of Karachi, Pakistan. Proc Pak Acad Sci. 2013;50:21–36.
Boudouresque CF, Verlaque M. Assessing scale and impact of ship-transported alien macrophytes in the Mediterranean Sea. In: Briand F, editor. Alien marine organisms introduced by ships in the Mediterranean and Black seas. Monaco: CIESM Workshop Monographs 20; 2002. p. 53–62.
Coppejans E, Leliaert F, Dargent O, Gunasekara R, De Clerck O. Abc Taxa. Sri Lankan Seaweeds Methodologies and field guide to the dominant species. Divisions of Algae from Sri Lanka and general remarks. Belgium. 2009;6:73–221.
Cormaci M, Furnari G, Catra M, Alongi G, Giaccone G. Marine benthic flora of the mediterranean: Phaeophyceae. Bollettine Accad Gioenia. 2012;45:1–508.
Farrant PA, King RJ. The Dictyotales of New South Wales. Proc Linnean Soc New South Wall. 1989;110:369–405.
Gaillard J. Monographic study of Padina tetrastromatica Hauck. Bulletin Fondamental Inst Black Afr Seri Sci Nat. 1967;29:447–63.
Galil BS, Zenetos A. Alien species in the Mediterranean Sea: which, when, where, why? Hydrobiologia. 2008;606:105–16.
Geraldino PJL, Lawrence ML, Boo SM. Morphological study of the marine algal genus Padina (Dictyotales, Phaeophyceae) from the southern Philippines: 3 species new to the Philippines. Algae. 2005;20:99–112.
Giaccone G. New and interesting species of Rhodophyceae from the eastern Mediterranean Sea. G Bot Ital. 1968;102:397–414.
Mayhoob H. Research of the marine vegetation at the Syrian coast. Experimental study on the morphogenesis and development of some species which less Known, PhD Thesis. France: University Caen; 1976. p. 286.
Mayhoob H. The invasion of the Syrian coast by the brown alga of the red sea. J Damascus Univ. 1989;5:65–79.
Mayhoob H, Billard C. Contribution of knowledge of Stypopodium Sp. installed at the Syrian coast. Cryptogamie Algology. 1991;12:125–36.
Mayhoob H. The presence of tropical alga Padina tetrastromatica Hauck near Latakia (Syria). J Damascus Univ. 2004;2:77–89.
Mayhoob H, Hatoum O. The presence of Cystoseira Balearica Sauv. Et C. barbatula Kg. Emend Cormaci et Al., Syria. J Tishreen Univ. 2005;27:207–18.
Ni-Ni-Win, Hanyuda T, Stefano GAD, Furnari G, Meinesz A, Kawai H. Padina ditristromatica sp. nov. and Padina pavonicoides sp. nov. (Dictyotales, Phaeophyceae), two new species from the Mediterranean Sea based on morphological and molecular markers. Eur J Phycology. 2011;46:327–41.
Occhipinti-Ambrogi A. Biotic invasions in a Mediterranean lagoon. J Biol Invasions. 2000;2:165–76.
Papenfuss GF. Review of the genera of Dictyotales (Phaeophycophyta). J Bulletin Japanese Soc Phycology. 1977;25:271–87.
Ribera MA, Go’mez-Garreta A, Gallardo T, Cormaci M, Furnari G, Giaccone G. Check-list of Mediterranean seaweeds. I. Fucophyceae (Warming 1884). J Bot Marina. 1992;35:109–30.
Streftaris NN, Zenetos A, Papathnassiou E. Globalistaion in marine ecosystems: the story of non-indigenous marine species across European seas. Greece. Oceanogr Mar Biol. 2005;43:419–53.
Taylor WR. Marine algae of the northeastern coast of North America. Ann Arbor: University of Michigan, Press; 1960.
UNEP/IUCN/GIS. Posidonia: Red Book “Gérard Vuignier”, marine plants, populations and landscapes threatened in the Mediterranean, MAP Technical Reports Series. No. 43. Athens: UNEP; 1990. p. 250. French only.
We thank Tishreen University for funding this project and the High Institute of Marine Research, Latakia for logistical support.